ZA200304331B - Organic compounds. - Google Patents
Organic compounds. Download PDFInfo
- Publication number
- ZA200304331B ZA200304331B ZA200304331A ZA200304331A ZA200304331B ZA 200304331 B ZA200304331 B ZA 200304331B ZA 200304331 A ZA200304331 A ZA 200304331A ZA 200304331 A ZA200304331 A ZA 200304331A ZA 200304331 B ZA200304331 B ZA 200304331B
- Authority
- ZA
- South Africa
- Prior art keywords
- halogen
- alkyl
- formula
- hydrogen
- compounds
- Prior art date
Links
- 150000002894 organic compounds Chemical class 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 66
- 229910052739 hydrogen Inorganic materials 0.000 claims description 57
- 239000001257 hydrogen Substances 0.000 claims description 57
- -1 phenyloxy Chemical group 0.000 claims description 40
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 37
- 125000001424 substituent group Chemical group 0.000 claims description 29
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 24
- 150000002367 halogens Chemical class 0.000 claims description 23
- 229910052736 halogen Inorganic materials 0.000 claims description 22
- 150000002431 hydrogen Chemical class 0.000 claims description 17
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 13
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 13
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 8
- 125000004104 aryloxy group Chemical group 0.000 claims description 7
- 241001465754 Metazoa Species 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 125000005554 pyridyloxy group Chemical group 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 4
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 4
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 244000144972 livestock Species 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 241000607479 Yersinia pestis Species 0.000 claims 4
- 240000007594 Oryza sativa Species 0.000 claims 2
- 244000045947 parasite Species 0.000 claims 2
- 244000294411 Mirabilis expansa Species 0.000 claims 1
- 235000015429 Mirabilis expansa Nutrition 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 235000013536 miso Nutrition 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 7
- 229910052794 bromium Inorganic materials 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 229910052801 chlorine Inorganic materials 0.000 description 7
- 229910052731 fluorine Inorganic materials 0.000 description 7
- 239000011737 fluorine Substances 0.000 description 7
- 125000001153 fluoro group Chemical group F* 0.000 description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 150000008361 aminoacetonitriles Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 244000079386 endoparasite Species 0.000 description 3
- 125000004438 haloalkoxy group Chemical group 0.000 description 3
- 125000001188 haloalkyl group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 244000000013 helminth Species 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 230000000361 pesticidal effect Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000006039 1-hexenyl group Chemical group 0.000 description 1
- 125000005978 1-naphthyloxy group Chemical group 0.000 description 1
- 125000004797 2,2,2-trichloroethoxy group Chemical group ClC(CO*)(Cl)Cl 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000005979 2-naphthyloxy group Chemical group 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241000244206 Nematoda Species 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000006193 alkinyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000005366 cycloalkylthio group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 description 1
- 125000005347 halocycloalkyl group Chemical group 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- FXWHFKOXMBTCMP-WMEDONTMSA-N milbemycin Natural products COC1C2OCC3=C/C=C/C(C)CC(=CCC4CC(CC5(O4)OC(C)C(C)C(OC(=O)C(C)CC(C)C)C5O)OC(=O)C(C=C1C)C23O)C FXWHFKOXMBTCMP-WMEDONTMSA-N 0.000 description 1
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical class O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 ZLBGSRMUSVULIE-GSMJGMFJSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/275—Nitriles; Isonitriles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/275—Nitriles; Isonitriles
- A61K31/277—Nitriles; Isonitriles having a ring, e.g. verapamil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
Landscapes
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Paper (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH24892000 | 2000-12-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200304331B true ZA200304331B (en) | 2004-04-28 |
Family
ID=4569596
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200304331A ZA200304331B (en) | 2000-12-20 | 2003-06-03 | Organic compounds. |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US7700656B2 (fr) |
| EP (1) | EP1392281B1 (fr) |
| JP (1) | JP2004521097A (fr) |
| KR (1) | KR100850252B1 (fr) |
| CN (1) | CN1531426A (fr) |
| AR (1) | AR035523A1 (fr) |
| AT (1) | ATE354360T1 (fr) |
| AU (2) | AU3458802A (fr) |
| BR (1) | BR0116326A (fr) |
| CA (1) | CA2432388C (fr) |
| CY (1) | CY1106509T1 (fr) |
| DE (1) | DE60126838T2 (fr) |
| DK (1) | DK1392281T3 (fr) |
| ES (1) | ES2281453T3 (fr) |
| MX (1) | MXPA03005701A (fr) |
| NZ (1) | NZ526538A (fr) |
| PT (1) | PT1392281E (fr) |
| RU (1) | RU2286775C2 (fr) |
| TW (1) | TWI292712B (fr) |
| WO (1) | WO2002049641A2 (fr) |
| ZA (1) | ZA200304331B (fr) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR035531A1 (es) | 2001-01-22 | 2004-06-02 | Novartis Ag | Composicion para el control de plagas endoparasiticas en ganados y animales domesticos, un metodo para su control y el uso de dicha composicion para la preparacion de medicamentos |
| AR036054A1 (es) | 2001-06-15 | 2004-08-04 | Novartis Ag | Uso de compuestos de aminoacetonitrilo para el control de plagas, una composicion y un proceso para dicho control y una composicion farmaceutica contra parasitos |
| WO2003004474A1 (fr) * | 2001-07-06 | 2003-01-16 | Syngenta Participations Ag | Aminoacetonitriles a action pesticide |
| AR037746A1 (es) | 2001-12-06 | 2004-12-01 | Novartis Ag | Compuestos derivados de amidoacetonitrilo, un procedimiento para su preparacion, un procedimiento para la preparacion de compuestos intermediarios, una composicion para combatir parasitos, un procedimiento para combatir dichos parasitos, y el empleo de dichos derivados para la preparacion de una com |
| TW200305556A (en) * | 2002-03-21 | 2003-11-01 | Novartis Ag | Organic compounds |
| TW200400932A (en) * | 2002-06-19 | 2004-01-16 | Novartis Ag | Organic compounds |
| TW200409760A (en) * | 2002-09-11 | 2004-06-16 | Novartis Ag | Organic compounds |
| GB0402677D0 (en) * | 2003-11-06 | 2004-03-10 | Novartis Ag | Organic compounds |
| AR049391A1 (es) * | 2004-06-10 | 2006-07-26 | Novartis Ag | Derivados de aminoacetonitrilo y su uso para controlar parasitos en animales de sangre caliente |
| WO2006043654A1 (fr) * | 2004-10-22 | 2006-04-27 | Nihon Nohyaku Co., Ltd. | Dérivé d’acétonitrile, agent de régulation d’organismes nuisibles, et méthode d’utilisation dudit agent |
| WO2006050887A1 (fr) * | 2004-11-09 | 2006-05-18 | Novartis Ag | Procede de preparation d'enantiomeres de composes d'amidoacetonitrile a partir de leurs racemates |
| WO2007017088A1 (fr) * | 2005-07-25 | 2007-02-15 | Novartis Ag | Composés amidonitrile |
| DE102006025874A1 (de) | 2006-06-02 | 2007-12-06 | Bayer Cropscience Ag | Alkoxyalkyl-substituierte cyclische Ketoenole |
| WO2008062005A1 (fr) * | 2006-11-24 | 2008-05-29 | Novartis Ag | Utilisation de composés d'aminoacétonitrile pour la lutte contre les endoparasites chez des animaux homéothermes |
| DK2118055T3 (da) | 2007-02-09 | 2013-11-04 | Zoetis Uk Ltd | Antiparasitmidler |
| MX2009008028A (es) * | 2007-02-21 | 2009-08-07 | Pfizer Ltd | Agentes antiparasitarios. |
| RS58416B1 (sr) | 2007-05-15 | 2019-04-30 | Merial Inc | Ariloazol-2-il cijanoetilamino jedinjenja, postupci dobijanja i postupci njihove primene |
| JP5614853B2 (ja) | 2008-10-21 | 2014-10-29 | メリアル リミテッド | チオアミド化合物、その製造方法及び使用方法 |
| AU2009313920B2 (en) | 2008-11-14 | 2014-10-23 | Boehringer Ingelheim Animal Health USA Inc. | Enantiomerically enriched aryloazol- 2 -yl cyanoethylamino paraciticidal compounds |
| UY33282A (es) * | 2010-03-25 | 2011-09-30 | Novartis Ag | Composiciones endoparasiticidas |
| BR112013021337B1 (pt) * | 2011-03-02 | 2019-09-03 | Nihon Nohyaku Co Ltd | composição compreendendo um derivado de carboxamida para uso no controle de endoparasitas |
| US9422276B2 (en) * | 2011-11-25 | 2016-08-23 | Bayer Intellectual Property Gmbh | Use of aryl and hetaryl carboxamides as endoparasiticides |
| AU2013219467B2 (en) * | 2012-02-14 | 2016-07-07 | Nippon Soda Co., Ltd. | Aryloxyacetamide compound and pesticide |
| EP3202397B1 (fr) * | 2012-08-06 | 2019-09-25 | Pitney Pharmaceuticals Pty Limited | Composés pour le traitement de maladies associées à la voie mtor |
| US8822689B2 (en) | 2012-09-19 | 2014-09-02 | Merial Limited | Aryloazol-2-yl cyanoethylamino compounds, method of making and method of using thereof |
| AR094961A1 (es) | 2013-03-15 | 2015-09-09 | Lilly Co Eli | 1-hidroxi-benzooxaboroles como agentes antiparasitarios |
| EP2821412A1 (fr) * | 2013-07-01 | 2015-01-07 | Universität Zürich | Dérivés de 2-cyano-2-aminobenzoate-propyl organométalliques et leur utilisation comme anthelminthiques |
| PL3043791T3 (pl) * | 2013-09-13 | 2019-08-30 | Pitney Pharmaceuticals Pty Limited | Środek przeciwnowotworowy zawierający związek aminoacetonitrylowy jako substancję czynną |
| EP3235815A1 (fr) | 2016-04-19 | 2017-10-25 | Philipps-Universität Marburg | Agents actifs contre les helminthes parasites |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3457294A (en) * | 1966-04-22 | 1969-07-22 | Abbott Lab | N-(substituted-benzoyl) aminoaceto- and aminopropionitriles |
| FR1520925A (fr) * | 1966-04-22 | 1968-04-12 | Abbott Lab | Nouveaux benzoylamino-nitriles |
| US4515731A (en) * | 1975-08-25 | 1985-05-07 | Monsanto Company | Asymmetric catalysis |
| GB8517279D0 (en) | 1985-07-08 | 1985-08-14 | Ici Plc | Benzamide derivatives |
| JP2994182B2 (ja) * | 1992-07-23 | 1999-12-27 | 石原産業株式会社 | アミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤 |
| US6239077B1 (en) * | 1998-05-01 | 2001-05-29 | Nihon Nohyaku Co., Ltd. | Aminoacetonitrile derivative agricultural and horticultural insecticide containing the same and use thereof |
| AR035531A1 (es) | 2001-01-22 | 2004-06-02 | Novartis Ag | Composicion para el control de plagas endoparasiticas en ganados y animales domesticos, un metodo para su control y el uso de dicha composicion para la preparacion de medicamentos |
| BR0209828A (pt) | 2001-05-15 | 2004-06-15 | Novartis Ag | Compostos orgânicos |
| AR036054A1 (es) | 2001-06-15 | 2004-08-04 | Novartis Ag | Uso de compuestos de aminoacetonitrilo para el control de plagas, una composicion y un proceso para dicho control y una composicion farmaceutica contra parasitos |
| WO2003004474A1 (fr) * | 2001-07-06 | 2003-01-16 | Syngenta Participations Ag | Aminoacetonitriles a action pesticide |
| AR038156A1 (es) * | 2002-01-21 | 2004-12-29 | Novartis Ag | Compuestos de amidoacetonitrilo, proceso para su preparacion, composicion para controlar los parasitos, y uso de estos compuestos para preparar una composicion farmaceutica |
-
2001
- 2001-12-18 US US10/433,811 patent/US7700656B2/en not_active Expired - Lifetime
- 2001-12-18 KR KR1020037007242A patent/KR100850252B1/ko not_active IP Right Cessation
- 2001-12-18 CN CNA018210155A patent/CN1531426A/zh active Pending
- 2001-12-18 AU AU3458802A patent/AU3458802A/xx active Pending
- 2001-12-18 RU RU2003122196/15A patent/RU2286775C2/ru active
- 2001-12-18 DK DK01985421T patent/DK1392281T3/da active
- 2001-12-18 MX MXPA03005701A patent/MXPA03005701A/es active IP Right Grant
- 2001-12-18 TW TW090131306A patent/TWI292712B/zh not_active IP Right Cessation
- 2001-12-18 NZ NZ526538A patent/NZ526538A/en not_active IP Right Cessation
- 2001-12-18 AR ARP010105864A patent/AR035523A1/es not_active Application Discontinuation
- 2001-12-18 AU AU2002234588A patent/AU2002234588B2/en not_active Expired
- 2001-12-18 AT AT01985421T patent/ATE354360T1/de active
- 2001-12-18 DE DE60126838T patent/DE60126838T2/de not_active Expired - Lifetime
- 2001-12-18 ES ES01985421T patent/ES2281453T3/es not_active Expired - Lifetime
- 2001-12-18 EP EP01985421A patent/EP1392281B1/fr not_active Expired - Lifetime
- 2001-12-18 BR BR0116326-4A patent/BR0116326A/pt not_active IP Right Cessation
- 2001-12-18 PT PT01985421T patent/PT1392281E/pt unknown
- 2001-12-18 JP JP2002550981A patent/JP2004521097A/ja active Pending
- 2001-12-18 WO PCT/EP2001/014926 patent/WO2002049641A2/fr active IP Right Grant
- 2001-12-18 CA CA2432388A patent/CA2432388C/fr not_active Expired - Lifetime
-
2003
- 2003-06-03 ZA ZA200304331A patent/ZA200304331B/en unknown
-
2007
- 2007-04-12 CY CY20071100511T patent/CY1106509T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATE354360T1 (de) | 2007-03-15 |
| RU2003122196A (ru) | 2005-03-20 |
| DE60126838T2 (de) | 2007-11-08 |
| NZ526538A (en) | 2005-12-23 |
| WO2002049641A2 (fr) | 2002-06-27 |
| BR0116326A (pt) | 2004-07-06 |
| DE60126838D1 (de) | 2007-04-05 |
| MXPA03005701A (es) | 2003-10-06 |
| WO2002049641A3 (fr) | 2003-12-04 |
| DK1392281T3 (da) | 2007-06-11 |
| CN1531426A (zh) | 2004-09-22 |
| AU3458802A (en) | 2002-07-01 |
| PT1392281E (pt) | 2007-05-31 |
| KR20030061414A (ko) | 2003-07-18 |
| US7700656B2 (en) | 2010-04-20 |
| AR035523A1 (es) | 2004-06-02 |
| AU2002234588B2 (en) | 2005-03-24 |
| ES2281453T3 (es) | 2007-10-01 |
| CA2432388A1 (fr) | 2002-06-27 |
| KR100850252B1 (ko) | 2008-08-04 |
| JP2004521097A (ja) | 2004-07-15 |
| CA2432388C (fr) | 2010-06-08 |
| EP1392281B1 (fr) | 2007-02-21 |
| RU2286775C2 (ru) | 2006-11-10 |
| CY1106509T1 (el) | 2012-01-25 |
| US20040082624A1 (en) | 2004-04-29 |
| TWI292712B (en) | 2008-01-21 |
| EP1392281A2 (fr) | 2004-03-03 |
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